(S)-Benzyl 4-((tert-butyldimethylsilyl)oxy)-2-hydroxybutanoate CAS 863000-09-3

Purity 97%+In StockPharmaceutical Standards
CAS No.863000-09-3
Molecular FormulaC17H28O4Si
Molecular Weight324.49 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(S)-Benzyl 4-((tert-butyldimethylsilyl)oxy)-2-hydroxybutanoate CAS 863000-09-3 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including (S)-Benzyl 4-((tert-butyldimethylsilyl)oxy)-2-hydroxybutanoate.

CATO supplies (S)-Benzyl 4-((tert-butyldimethylsilyl)oxy)-2-hydroxybutanoate (CAS 863000-09-3), a certified reference material (molecular formula C17H28O4Si, MW 324.49 g/mol) for analytical method development and quality control.

The molecular framework of (S)-Benzyl 4-((tert-butyldimethylsilyl)oxy)-2-hydroxybutanoate (C17H28O4Si) is characterized by a steroid core, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), (S)-Benzyl 4-((tert-butyldimethylsilyl)oxy)-2-hydroxybutanoate meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC17H28O4Si
Molecular Weight324.49 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at room temperature, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987

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